Abstract: TH-PO1007
From Ovarian Hyperstimulation Syndrome (OHSS) to Cortical Necrosis: A Rare Renal Catastrophe
Session Information
- Women's Health and Kidney Diseases
November 06, 2025 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Women's Health and Kidney Diseases
- 2200 Women's Health and Kidney Diseases
Authors
- Kolluru, Eshwar Chowdari, All India Institute of Medical Sciences New Delhi, New Delhi, DL, India
- Subbiah, Arunkumar, All India Institute of Medical Sciences New Delhi, New Delhi, DL, India
- Bhowmik, Dipankar M., All India Institute of Medical Sciences New Delhi, New Delhi, DL, India
Introduction
Ovarian hyperstimulation syndrome (OHSS) is a known complication of assisted reproduction. While typically mild and self-limiting, critical OHSS can cause anasarca and multi-organ dysfunction. Acute kidney injury (AKI) is an uncommon complication of OHSS, with cortical necrosis being even rarer. We present a case of critical OHSS leading to acute cortical necrosis in a young woman with no prior comorbidities, highlighting the importance of early detection and aggressive supportive care.
Case Description
A 26-year-old woman with primary infertility underwent controlled ovarian stimulation using rFSH, hCG, and cetrorelix. Seven oocytes were retrieved. Within three days, she developed abdominal pain, distension, and respiratory distress and presented to our center with oliguria and multi-organ dysfunction. Examination showed pallor, pedal edema, hypotension, & hypoxia. Labs revealed severe thrombocytopenia, metabolic acidosis, renal dysfunction, elevated transaminases, & hypoalbuminemia. Ultrasound showed bilaterally enlarged echogenic kidneys and gross ascites. She was managed with IV albumin, supportive care, and intermittent hemodialysis. Inotropes were tapered in 48 hours, with clinical improvement over a week, though she remained oligo-anuric. A diagnosis of critical OHSS was made with differentials of acute tubular necrosis (ATN) and thrombotic microangiopathy (TMA). Sepsis, infections, TMA, and autoimmune causes were ruled out. Renal biopsy confirmed acute cortical necrosis. She remains on RRT and is under OPD follow-up, with plans for renal transplantation.
Discussion
Critical OHSS, seen in 0.1–2% of cases, can be fatal due to cytokine-mediated vascular permeability, causing edema, hemoconcentration, and organ hypoperfusion. ATN or prerenal factors primarily cause AKI in OHSS. In reproductive-age females, cortical necrosis is typically obstetric in origin—septic abortion, eclampsia, or sepsis—making OHSS a rare cause. This case is notable as it developed without typical risk factors like high estradiol, early pregnancy, or prior OHSS. Only two prior cases of OHSS-related cortical necrosis have been reported. Prompt initiation of fluids, albumin, vasopressors, and RRT is critical for managing this condition. With the increasing use of assisted reproduction, vigilant monitoring during ovarian stimulation is vital to prevent such outcomes.